A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065335



Internal ID21974568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161041747..161041747hg38UCSC Ensembl
chr3:160759535..160759535hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547275
Samples
Known GenesPPM1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065335
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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